aplasia cutis congenita over the scalp vertex Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in the congenital absence of skin on the scalp vertex, often just lateral to the midline. (Human Phenotype Ontology, HP_0004471)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004471
Similar Terms
Downloads & Tools

Genes

1 genes associated with the aplasia cutis congenita over the scalp vertex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMS1 BMS1 ribosome biogenesis factor